Canonical Allele Identifier: CA6243501

Gene: PGR

Linked Data

• dbSNP Id: rs149186732
• ExAC: 11:100922293 C / T
• gnomAD v2: 11-100922293-C-T
• gnomAD v3: 11-101051562-C-T
• gnomAD v4: 11-101051562-C-T
• COSMIC: COSM53395 ; COSM4183266
• MyVariant Identifiers: chr11:g.100922293C>T (hg19) ; chr11:g.101051562C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.101051562C>T , CM000673.2:g.101051562C>T	GRCh38
NC_000011.9:g.100922293C>T , CM000673.1:g.100922293C>T	GRCh37
NC_000011.8:g.100427503C>T	NCBI36
NG_016475.1:g.83252G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325455.10:c.2219G>A MANE Select	ENSP00000325120.5:p.Arg740Gln
ENST00000263463.9:c.1913G>A	ENSP00000263463.5:p.Arg638Gln
ENST00000325455.9:c.2219G>A	ENSP00000325120.5:p.Arg740Gln
ENST00000526300.5:c.1913G>A	ENSP00000436803.1:p.Arg638Gln
ENST00000528960.5:c.2102G>A	ENSP00000432914.1:p.Arg701Gln
ENST00000533207.5:n.1586G>A
ENST00000534013.5:c.437G>A	ENSP00000436561.1:p.Arg146Gln
ENST00000534780.5:c.2219G>A	ENSP00000432352.1:p.Arg740Gln
ENST00000617858.4:c.1913G>A	ENSP00000481227.1:p.Arg638Gln
ENST00000619228.2:c.2102G>A	ENSP00000482698.1:p.Arg701Gln
NM_000926.4:c.2219G>A MANE Select	NP_000917.3:p.Arg740Gln
NM_001202474.3:c.1727G>A	NP_001189403.1:p.Arg576Gln
NM_001271161.2:c.1421G>A	NP_001258090.1:p.Arg474Gln
NM_001271162.1:c.437G>A	NP_001258091.1:p.Arg146Gln
NR_073141.2:n.2212G>A
NR_073142.2:n.2095G>A
NR_073143.2:n.1906G>A
XM_006718858.2:c.2219G>A	XP_006718921.1:p.Arg740Gln
XR_947831.1:n.3900G>A
XM_006718858.3:c.2219G>A	XP_006718921.1:p.Arg740Gln
NM_001271162.2:c.437G>A	NP_001258091.1:p.Arg146Gln
NR_073141.3:n.2226G>A
NR_073142.3:n.2109G>A
NR_073143.3:n.1920G>A